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丙酸倍氯米松气雾剂用于常年性鼻炎。

Beclomethasone dipropionate aerosol in perennial rhinitis.

作者信息

Tarlo S M, Cockcroft D W, Dolovich J, Hargreave F E

出版信息

J Allergy Clin Immunol. 1977 Mar;59(3):232-6. doi: 10.1016/0091-6749(77)90155-5.

Abstract

Beclomethasone dipropionate aerosol (BDA), 50 mug four times daily sprayed into each nostril, was compared with placebo in a double-blind crossover trial in 26 patients with perennial rhinitis. Patients received BDA for 3 weeks and placebo for 3 weeks; the order of administration was randomized. Response was assessed with daily symptom score cards and twice weekly measurements of nasal airway inspiratory resistance at a standard flow rate of 0.4 L/sec. Symptom score and nasal resistance during BDA treatment were significantly lower than those duirng placebo treatment (p less than 0.02 and p less than 0.05, respectively) in the third week. Eighteen of the patients expressed a preference for BDA, 6 for placebo, and 2 for neither (p less than 0.05). Acceptable symptomatic improvement (moderate or marked) was achieved by 54%. Mild side effects were noted by 5 patients; these included nasal irritation and bleeding in 2, aerosol-induced sneezing in 2, and headache in 1. These side effects occurred in 3 patients who used BDA, 1 who used placebo, and 1 who used both. After a 6-mo follow-up period, in which the dose of BDA was adjusted and concurrent initial oral prednisone was administered to patients who were treatment failures, 73% of the patients obtained moderate or marked symptomatic improvement. No further side effects were noted during this time. Results in those in whom a possible allergic component could be identified were not different from those of the whole group. We conclude that BDA is a useful addition to the therapy of perennial rhinitis.

摘要

在一项针对26例常年性鼻炎患者的双盲交叉试验中,将丙酸倍氯米松气雾剂(BDA),每日4次,每次50微克喷入每个鼻孔,与安慰剂进行了比较。患者接受BDA治疗3周,安慰剂治疗3周;给药顺序随机。通过每日症状评分卡以及每周两次以0.4升/秒的标准流速测量鼻气道吸气阻力来评估反应。在第三周,BDA治疗期间的症状评分和鼻阻力显著低于安慰剂治疗期间(分别为p<0.02和p<0.05)。18例患者表示更喜欢BDA,6例更喜欢安慰剂,2例无偏好(p<0.05)。54%的患者实现了可接受的症状改善(中度或显著)。5例患者出现轻度副作用;其中2例包括鼻刺激和出血,2例气雾剂诱发的打喷嚏,1例头痛。这些副作用发生在3例使用BDA的患者、1例使用安慰剂的患者和1例两者都使用的患者中。在6个月的随访期内,调整了BDA剂量,并对治疗失败的患者同时给予初始口服泼尼松,73%的患者获得了中度或显著的症状改善。在此期间未发现进一步的副作用。在那些可识别出可能过敏成分的患者中,结果与整个组的结果没有差异。我们得出结论,BDA是常年性鼻炎治疗中的一种有用补充药物。

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